Incidental Mutation 'R2002:Hjurp'
| ID |
223125 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Hjurp
|
| Ensembl Gene |
ENSMUSG00000044783 |
| Gene Name |
Holliday junction recognition protein |
| Synonyms |
A730008H23Rik, C330011F01Rik, 6430706D22Rik |
| MMRRC Submission |
040012-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.915)
|
| Stock # |
R2002 (G1)
|
| Quality Score |
217 |
|
Status
|
Validated
|
| Chromosome |
1 |
| Chromosomal Location |
88190193-88205355 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
GT to GTT
at 88194246 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000118659
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054674]
[ENSMUST00000061013]
[ENSMUST00000065420]
[ENSMUST00000113130]
[ENSMUST00000127446]
[ENSMUST00000147393]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably null
Transcript: ENSMUST00000054674
|
| SMART Domains |
Protein: ENSMUSP00000054263
Gene: ENSMUSG00000044783
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Scm3
|
11 |
68 |
1.5e-10 |
PFAM |
|
low complexity region
|
159 |
175 |
N/A |
INTRINSIC |
|
low complexity region
|
215 |
232 |
N/A |
INTRINSIC |
|
Pfam:HJURP_mid
|
254 |
370 |
7.6e-54 |
PFAM |
|
Pfam:HJURP_C
|
385 |
446 |
3.1e-26 |
PFAM |
|
low complexity region
|
496 |
515 |
N/A |
INTRINSIC |
|
Pfam:HJURP_C
|
527 |
585 |
7.1e-21 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000061013
|
| SMART Domains |
Protein: ENSMUSP00000130508
Gene: ENSMUSG00000079429
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
9 |
26 |
N/A |
INTRINSIC |
|
low complexity region
|
99 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
1235 |
1248 |
N/A |
INTRINSIC |
|
SCOP:d1jdha_
|
1371 |
1669 |
9e-8 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000065420
|
| SMART Domains |
Protein: ENSMUSP00000070419
Gene: ENSMUSG00000044783
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Scm3
|
9 |
70 |
2.9e-11 |
PFAM |
|
low complexity region
|
83 |
99 |
N/A |
INTRINSIC |
|
low complexity region
|
139 |
156 |
N/A |
INTRINSIC |
|
Pfam:HJURP_mid
|
178 |
295 |
7.4e-64 |
PFAM |
|
Pfam:HJURP_C
|
309 |
371 |
1.2e-26 |
PFAM |
|
low complexity region
|
420 |
439 |
N/A |
INTRINSIC |
|
Pfam:HJURP_C
|
451 |
510 |
3e-26 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000113130
|
| SMART Domains |
Protein: ENSMUSP00000108755
Gene: ENSMUSG00000079429
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
9 |
26 |
N/A |
INTRINSIC |
|
low complexity region
|
99 |
112 |
N/A |
INTRINSIC |
|
low complexity region
|
1232 |
1245 |
N/A |
INTRINSIC |
|
SCOP:d1gw5a_
|
1446 |
1671 |
6e-6 |
SMART |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000127446
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000128532
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000147393
|
| SMART Domains |
Protein: ENSMUSP00000120753
Gene: ENSMUSG00000044783
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:Scm3
|
9 |
70 |
7.2e-13 |
PFAM |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148384
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.2%
- 20x: 91.6%
|
| Validation Efficiency |
97% (72/74) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 75 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930548G14Rik |
T |
C |
15: 46,489,002 (GRCm39) |
|
noncoding transcript |
Het |
| Abcb4 |
T |
A |
5: 8,955,989 (GRCm39) |
S98T |
probably benign |
Het |
| Acan |
T |
C |
7: 78,750,541 (GRCm39) |
S1771P |
probably damaging |
Het |
| Acvr1c |
T |
A |
2: 58,205,987 (GRCm39) |
Q41L |
probably benign |
Het |
| Ak2 |
T |
A |
4: 128,902,022 (GRCm39) |
S232T |
probably benign |
Het |
| Akr1e1 |
T |
A |
13: 4,657,564 (GRCm39) |
|
probably benign |
Het |
| Ano7 |
T |
C |
1: 93,328,303 (GRCm39) |
|
probably benign |
Het |
| Aox1 |
T |
A |
1: 58,086,300 (GRCm39) |
H68Q |
possibly damaging |
Het |
| Apaf1 |
A |
G |
10: 90,897,676 (GRCm39) |
V269A |
possibly damaging |
Het |
| Apba2 |
A |
T |
7: 64,383,290 (GRCm39) |
I368F |
probably damaging |
Het |
| Armc3 |
A |
G |
2: 19,293,747 (GRCm39) |
M513V |
probably benign |
Het |
| Asb5 |
G |
A |
8: 55,036,655 (GRCm39) |
V116M |
probably damaging |
Het |
| Atg16l2 |
A |
G |
7: 100,944,127 (GRCm39) |
S280P |
possibly damaging |
Het |
| Atp6v0c |
G |
T |
17: 24,383,835 (GRCm39) |
T40K |
probably damaging |
Het |
| Cdk2ap2 |
A |
G |
19: 4,147,903 (GRCm39) |
M57V |
possibly damaging |
Het |
| Cip2a |
T |
C |
16: 48,826,214 (GRCm39) |
|
probably benign |
Het |
| Ctnnd1 |
T |
C |
2: 84,450,704 (GRCm39) |
N172S |
probably benign |
Het |
| Ddx55 |
T |
A |
5: 124,704,503 (GRCm39) |
V370E |
probably damaging |
Het |
| Ddx6 |
A |
G |
9: 44,518,831 (GRCm39) |
T48A |
probably benign |
Het |
| Dnah10 |
C |
T |
5: 124,911,052 (GRCm39) |
R4490W |
probably damaging |
Het |
| Dspp |
T |
A |
5: 104,326,425 (GRCm39) |
S929R |
unknown |
Het |
| Erbb3 |
T |
C |
10: 128,422,094 (GRCm39) |
Y50C |
probably benign |
Het |
| Fam209 |
C |
A |
2: 172,314,689 (GRCm39) |
N59K |
probably benign |
Het |
| Fgd3 |
T |
C |
13: 49,449,931 (GRCm39) |
E106G |
probably benign |
Het |
| Frmd4a |
A |
C |
2: 4,577,176 (GRCm39) |
K344T |
probably damaging |
Het |
| Gbe1 |
A |
G |
16: 70,325,814 (GRCm39) |
E617G |
probably damaging |
Het |
| Gm5089 |
T |
A |
14: 122,673,686 (GRCm39) |
I12F |
unknown |
Het |
| Gm7052 |
T |
A |
17: 22,258,920 (GRCm39) |
|
probably benign |
Het |
| Gria1 |
A |
T |
11: 56,902,930 (GRCm39) |
N24I |
possibly damaging |
Het |
| Grin2b |
T |
C |
6: 135,710,243 (GRCm39) |
E1101G |
probably damaging |
Het |
| Kcnma1 |
A |
C |
14: 23,387,097 (GRCm39) |
S982A |
probably damaging |
Het |
| Khdrbs3 |
T |
A |
15: 68,885,328 (GRCm39) |
|
probably benign |
Het |
| Kif23 |
A |
T |
9: 61,834,666 (GRCm39) |
C426* |
probably null |
Het |
| Lmo7 |
G |
T |
14: 102,124,497 (GRCm39) |
A319S |
probably benign |
Het |
| Ly6c1 |
T |
A |
15: 74,920,342 (GRCm39) |
T7S |
possibly damaging |
Het |
| Magel2 |
G |
A |
7: 62,028,844 (GRCm39) |
V583I |
unknown |
Het |
| Mamdc4 |
A |
T |
2: 25,457,244 (GRCm39) |
W548R |
probably damaging |
Het |
| Mfsd2a |
C |
T |
4: 122,850,609 (GRCm39) |
R88Q |
probably damaging |
Het |
| Mkrn1 |
T |
C |
6: 39,382,737 (GRCm39) |
T158A |
probably benign |
Het |
| Mroh2b |
G |
T |
15: 4,955,166 (GRCm39) |
D720Y |
probably damaging |
Het |
| Mycbp2 |
A |
G |
14: 103,485,839 (GRCm39) |
V1041A |
probably damaging |
Het |
| Ncam2 |
A |
T |
16: 81,386,586 (GRCm39) |
H655L |
possibly damaging |
Het |
| Npas2 |
T |
C |
1: 39,377,276 (GRCm39) |
V546A |
probably benign |
Het |
| Nrxn3 |
G |
A |
12: 90,299,089 (GRCm39) |
A400T |
probably damaging |
Het |
| Oog3 |
G |
T |
4: 143,884,675 (GRCm39) |
H420Q |
possibly damaging |
Het |
| Or3a10 |
A |
T |
11: 73,935,865 (GRCm39) |
S78R |
possibly damaging |
Het |
| Or5ap2 |
T |
A |
2: 85,680,744 (GRCm39) |
V316E |
probably benign |
Het |
| Or8k28 |
T |
C |
2: 86,285,817 (GRCm39) |
H266R |
probably benign |
Het |
| Pak5 |
T |
A |
2: 135,958,557 (GRCm39) |
H177L |
probably benign |
Het |
| Pcca |
A |
G |
14: 123,124,477 (GRCm39) |
I683V |
probably benign |
Het |
| Pea15a |
T |
C |
1: 172,026,252 (GRCm39) |
I90V |
probably benign |
Het |
| Plagl1 |
C |
A |
10: 13,004,402 (GRCm39) |
|
probably benign |
Het |
| Prmt1 |
A |
G |
7: 44,628,148 (GRCm39) |
V237A |
probably damaging |
Het |
| Ptprz1 |
T |
A |
6: 23,027,833 (GRCm39) |
Y910* |
probably null |
Het |
| Rasal3 |
T |
A |
17: 32,612,585 (GRCm39) |
T757S |
probably damaging |
Het |
| Rbbp8 |
T |
C |
18: 11,860,223 (GRCm39) |
|
probably benign |
Het |
| S1pr1 |
A |
G |
3: 115,506,544 (GRCm39) |
S17P |
probably benign |
Het |
| Scel |
G |
A |
14: 103,779,421 (GRCm39) |
V131M |
probably damaging |
Het |
| Scn2a |
G |
A |
2: 65,512,427 (GRCm39) |
R188Q |
probably null |
Het |
| Snap29 |
T |
A |
16: 17,224,190 (GRCm39) |
Y68* |
probably null |
Het |
| Spdl1 |
T |
C |
11: 34,713,473 (GRCm39) |
T199A |
probably benign |
Het |
| Srbd1 |
T |
C |
17: 86,449,828 (GRCm39) |
N14D |
probably benign |
Het |
| Ston1 |
G |
A |
17: 88,942,957 (GRCm39) |
G121D |
probably benign |
Het |
| Syt16 |
G |
A |
12: 74,281,977 (GRCm39) |
G367E |
possibly damaging |
Het |
| Tdpoz1 |
T |
C |
3: 93,578,710 (GRCm39) |
T25A |
possibly damaging |
Het |
| Tmem182 |
T |
A |
1: 40,845,355 (GRCm39) |
Y77N |
probably damaging |
Het |
| Tmprss11f |
A |
T |
5: 86,687,627 (GRCm39) |
|
probably benign |
Het |
| Trp73 |
T |
C |
4: 154,165,902 (GRCm39) |
T56A |
probably damaging |
Het |
| Trpm3 |
A |
G |
19: 22,959,947 (GRCm39) |
K1194R |
probably damaging |
Het |
| Ttc39c |
T |
A |
18: 12,830,935 (GRCm39) |
|
probably null |
Het |
| Ube4b |
T |
C |
4: 149,468,254 (GRCm39) |
D174G |
probably benign |
Het |
| Vmn1r211 |
A |
T |
13: 23,035,953 (GRCm39) |
M238K |
probably damaging |
Het |
| Wsb2 |
T |
A |
5: 117,508,798 (GRCm39) |
N77K |
probably benign |
Het |
| Xkr4 |
C |
T |
1: 3,741,318 (GRCm39) |
R85Q |
probably benign |
Het |
| Zmynd11 |
T |
A |
13: 9,739,514 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Hjurp |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00990:Hjurp
|
APN |
1 |
88,197,991 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL03099:Hjurp
|
APN |
1 |
88,194,011 (GRCm39) |
missense |
probably benign |
0.09 |
|
BB003:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL03097:Hjurp
|
UTSW |
1 |
88,194,002 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL03098:Hjurp
|
UTSW |
1 |
88,194,002 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL03147:Hjurp
|
UTSW |
1 |
88,194,002 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4131001:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4142001:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4142001:Hjurp
|
UTSW |
1 |
88,193,768 (GRCm39) |
missense |
probably damaging |
0.98 |
|
PIT4142001:Hjurp
|
UTSW |
1 |
88,194,338 (GRCm39) |
missense |
probably benign |
0.04 |
|
PIT4142001:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4378001:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4812001:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R0053:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R0371:Hjurp
|
UTSW |
1 |
88,205,090 (GRCm39) |
splice site |
probably benign |
|
|
R0442:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R0762:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R0928:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R1333:Hjurp
|
UTSW |
1 |
88,193,768 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1342:Hjurp
|
UTSW |
1 |
88,205,090 (GRCm39) |
splice site |
probably benign |
|
|
R1364:Hjurp
|
UTSW |
1 |
88,194,247 (GRCm39) |
frame shift |
probably null |
|
|
R1496:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R1637:Hjurp
|
UTSW |
1 |
88,193,843 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1905:Hjurp
|
UTSW |
1 |
88,194,338 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1965:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R1992:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2023:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2024:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2332:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R2420:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2422:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R2869:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2870:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2871:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R2872:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3019:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3021:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3150:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R3411:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3552:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3704:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R3730:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3733:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3764:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3799:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R3819:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R3857:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3930:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R3952:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R4090:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R4159:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R4207:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R4322:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R4391:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4392:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R4393:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R4393:Hjurp
|
UTSW |
1 |
88,194,283 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R4397:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R4700:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R4808:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R4900:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R4901:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5023:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R5024:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R5076:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5123:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R5236:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5300:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5318:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5370:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5410:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5445:Hjurp
|
UTSW |
1 |
88,194,038 (GRCm39) |
missense |
probably benign |
0.43 |
|
R5457:Hjurp
|
UTSW |
1 |
88,194,247 (GRCm39) |
frame shift |
probably null |
|
|
R5497:Hjurp
|
UTSW |
1 |
88,194,042 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R5560:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5561:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5615:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R5661:Hjurp
|
UTSW |
1 |
88,204,937 (GRCm39) |
splice site |
probably benign |
|
|
R5722:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R6087:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R6089:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R6090:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R6125:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R6175:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R6362:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R6659:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R7016:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R7016:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R7045:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R7179:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R7200:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R7463:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R7912:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R8215:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R8968:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9038:Hjurp
|
UTSW |
1 |
88,194,246 (GRCm39) |
nonsense |
probably null |
|
|
R9115:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9133:Hjurp
|
UTSW |
1 |
88,202,772 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R9146:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9221:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9475:Hjurp
|
UTSW |
1 |
88,193,999 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9482:Hjurp
|
UTSW |
1 |
88,193,996 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9565:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
R9599:Hjurp
|
UTSW |
1 |
88,194,000 (GRCm39) |
utr 3 prime |
probably benign |
|
|
V5622:Hjurp
|
UTSW |
1 |
88,205,247 (GRCm39) |
unclassified |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CCAGCTCTGGTTGATGTAGG -3'
(R):5'- ACTGTCATGGTTTGTGATGCCC -3'
Sequencing Primer
(F):5'- AGGTCTTGGTGGAGATGATGCAG -3'
(R):5'- CCTGCCCGGTGGGTAAGTATG -3'
|
| Posted On |
2014-08-25 |
Incidental Mutation